@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_head
{
this:
np:hasAssertion
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_assertion
;
np:hasProvenance
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_assertion
a
np:Assertion
.
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_provenance
a
np:Provenance
.
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_assertion
{
miriam-gene:2521
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGN2f4295b6e582bc0e01f88d8b171ceb94
sio:SIO_000628
miriam-gene:2521
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_provenance
{
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_assertion
dcterms:description
"[The SVA may therefore contribute to the modulation of FUS expression exhibited in and associated with neurological disorders including ALS where FUS regulation may be an important parameter in progression of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:24608899
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP414137.RAYaeSw8rMAz07iCuAq6kkbEH9E08rHWr6UMV_l1my_OQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:41+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}